510(k) Report

510(k) · Cleared

Cleared

EzOrtho

K211793510(k) TraditionalCleared Aug 23, 202174-day reviewClass II21 CFR 892.2050

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Ewoosoft Co., Ltd. · LLZ System, Image Processing, Radiological

Cleared on Aug 23, 2021 as substantially equivalent to K202948 (Ewoosoft Co., Ltd., 2020) after a 74-day review. Its family tree reaches back 9 generations to 1993. 5 later devices descend from it.

Decided
Aug 23, 2021
Review
74 days
Class
Class II
Product code
LLZ
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K930527 (1993). 10 ancestors in all. 5 later devices descend from it, 1 citing it directly.

  1. Root · 9 generations backK930527 Dental LinkEscan, Inc. · 1993
  2. 5 generations between
  3. 3 generations backK173094 OrthoVisionEwoosoft Co., Ltd. · 2017
  4. 2 generations backK192888 EzOrthoEwoosoft Co., Ltd. · 2020
  5. 1 generation backK202948 EzOrthoEwoosoft Co., Ltd. · 2020
  6. This deviceK211793 EzOrthoEwoosoft Co., Ltd. · 2021
  7. Descendant · cites it directly · 4 of its ownK220003 EzOrtho v1.3Ewoosoft Co., Ltd. · 2022
  8. Descendant · 2 generations on · 3 of its ownK222054 Denti.AI Auto-ChartDenti.Ai Technology, Inc. · 2022
  9. Descendant · 3 generations on · 2 of its ownK233590 Overjet Charting AssistOverjet, Inc. · 2024
  10. Descendant · 4 generations on · 1 of its ownK241684 Overjet Charting AssistOverjet, Inc. · 2024
  11. Descendant · 5 generations on · 0 of its ownK261059 Overjet Multi-Image Caries and Charting AssistOverjet, Inc. · 2026
Show all 9 generations
  1. Root · 9 generations backK930527 Dental LinkEscan, Inc. · 1993
  2. 8 generations backK955237 Tigerscan/TigerviewTau Corp. · 1996
  3. 7 generations backK012439 Dentaleye 2 Dental Image Management SystemRadco Data AB · 2002
  4. 6 generations backK043104 Kodak Orthodontic Imaging and Oms Imaging 8.0Practiceworks, Inc. · 2005
  5. 5 generations backK122427 CS Orthodontic Imaging Software CS Oms Imaging SoftwareCarestream Dental, LLC · 2012
  6. 4 generations backK131570 OrthovisionEwoosoft Co., Ltd. · 2013
  7. 3 generations backK173094 OrthoVisionEwoosoft Co., Ltd. · 2017
  8. 2 generations backK192888 EzOrthoEwoosoft Co., Ltd. · 2020
  9. 1 generation backK202948 EzOrthoEwoosoft Co., Ltd. · 2020
  10. This deviceK211793 EzOrthoEwoosoft Co., Ltd. · 2021

Most influential descendants

Showing 5 of 5 · See all
  • K220003EzOrtho v1.3Ewoosoft Co., Ltd. · 2022 · cites it directly4descendants
  • K222054Denti.AI Auto-ChartDenti.Ai Technology, Inc. · 2022 · 2 generations on3descendants
  • K233590Overjet Charting AssistOverjet, Inc. · 2024 · 3 generations on2descendants
  • K241684Overjet Charting AssistOverjet, Inc. · 2024 · 4 generations on1descendant
  • K261059Overjet Multi-Image Caries and Charting AssistOverjet, Inc. · 2026 · 5 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K930527Dental LinkEscan, Inc.1993—
−8K955237Tigerscan/TigerviewTau Corp.1996—
−7K012439Dentaleye 2 Dental Image Management SystemRadco Data AB2002—
−6K043104Kodak Orthodontic Imaging and Oms Imaging 8.0Practiceworks, Inc.2005—
−5K122427CS Orthodontic Imaging Software CS Oms Imaging SoftwareCarestream Dental, LLC2012—
−4K131570OrthovisionEwoosoft Co., Ltd.2013—
−3K173094OrthoVisionEwoosoft Co., Ltd.2017—
−2K192888EzOrthoEwoosoft Co., Ltd.2020—
−1K202948EzOrthoEwoosoft Co., Ltd.2020—
0 (this device)K211793EzOrthoEwoosoft Co., Ltd.2021—
+1K220003EzOrtho v1.3Ewoosoft Co., Ltd.2022—
+2K222054Denti.AI Auto-ChartDenti.Ai Technology, Inc.2022—
+3K233590Overjet Charting AssistOverjet, Inc.2024—
+4K241684Overjet Charting AssistOverjet, Inc.2024—
+5K261059Overjet Multi-Image Caries and Charting AssistOverjet, Inc.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202220
202420
202610
FIG. 1 — Lineage of K211793, 1993–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in LLZ? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new LLZ device

  1. #1 K230955 syngo Application Softwarescore 21.5 · 11 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K202948EzOrtho
Summary page 4
…gulatory Class: Class II • Product Code: LLZ 5. Predicate Device: • Manufacturer: Ewoosoft Co., Ltd. • Trade/Device name: EzOrtho • 510(k) number: K202948 • Regulation number 21 CFR 892.2050 • Regulation name: Picture Archiving and Communications System • Regulatory Cl…
Ewoosoft Co., Ltd.2020—

What descends from it? (5)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K220003EzOrtho v1.3Ewoosoft Co., Ltd.20224

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 28 years and passes through 6 companies; a new generation was cleared every 2.8 years on median.
  • None of the 10 ancestors has a recall.
  • Of its descendants, K220003 (Ewoosoft Co., Ltd., 2022) has gone furthest, with 4 descendants of its own.

How does its category compare?

All LLZ devices

LLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.

FDA decisions per year · LLZ

58in 2025

2007: 762008: 942009: 702010: 512011: 1062012: 822013: 952014: 782015: 642016: 822017: 782018: 1042019: 742020: 812021: 832022: 652023: 872024: 622025: 582026 (partial year): 45
2007high 106 (2011) · low 51 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LLZ

173in 2025

2007: 36 days median2008: 52 days median2009: 62 days median2010: 98 days median2011: 79 days median2012: 87 days median2013: 84 days median2014: 89 days median2015: 90 days median2016: 90 days median2017: 107 days median2018: 105 days median2019: 107 days median2020: 115 days median2021: 116 days median2022: 137 days median2023: 157 days median2024: 131 days median2025: 173 days median2026 (partial year): 110 days median
2007high 173 (2025) · low 36 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · LLZ

11in 2025

2007: 202008: 322009: 212010: 172011: 302012: 122013: 642014: 62015: 162016: 122017: 52018: 72019: 22020: 62021: 32022: 42023: 82024: 62025: 112026 (partial year): 14
2007high 64 (2013) · low 2 (2019)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LLZ

116in 2025

2007: 1522008: 1542009: 1452010: 1452011: 4542012: 2662013: 1,1302014: 15,6312015: 2112016: 2902017: 1042018: 722019: 882020: 822021: 702022: 282023: 262024: 422025: 116
2007high 15,631 (2014) · low 26 (2023)2025

MAUDE reports naming product code LLZ, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007763620152
2008945232154
2009706221145
2010519817145
20111067930454
2012828712266
20139584641,130
20147889615,631
2015649016211
2016829012290
2017781075104
2018104105772
201974107288
202081115682
202183116370
202265137428
202387157826
202462131642
20255817311116
20264511014—

What is it indicated for?

EzOrtho is a software indicated for use by dentists who provide orthodontic treatment for image analysis, simulation, profilogram, VTO/STO and patient consultation. Results produced by the software's diagnostic, treatment planning and simulation tools are dependent on the interpretation of trained and licensed practitioners or dentists.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K211793: EzOrtho.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K211793

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026